200 related articles for article (PubMed ID: 15517821)
1. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
Lukusa T; Vermeesch JR; Holvoet M; Fryns JP; Devriendt K
Genet Couns; 2004; 15(3):293-301. PubMed ID: 15517821
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.
Smith M; Escamilla JR; Filipek P; Bocian ME; Modahl C; Flodman P; Spence MA
Cytogenet Cell Genet; 2001; 94(1-2):15-22. PubMed ID: 11701947
[TBL] [Abstract][Full Text] [Related]
3. Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH.
Goizet C; Excoffier E; Taine L; Taupiac E; El Moneim AA; Arveiler B; Bouvard M; Lacombe D
Am J Med Genet; 2000 Dec; 96(6):839-44. PubMed ID: 11121193
[TBL] [Abstract][Full Text] [Related]
4. Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
Maddox LO; Menold MM; Bass MP; Rogala AR; Pericak-Vance MA; Vance JM; Gilbert JR
Genomics; 1999 Dec; 62(3):325-31. PubMed ID: 10644429
[TBL] [Abstract][Full Text] [Related]
5. Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expression.
Wakui K; Toyoda A; Kubota T; Hidaka E; Ishikawa M; Katsuyama T; Sakaki Y; Hattori M; Fukushima Y
J Hum Genet; 2002; 47(10):511-6. PubMed ID: 12376739
[TBL] [Abstract][Full Text] [Related]
6. Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.
Cargile CB; Goh DL; Goodman BK; Chen XN; Korenberg JR; Semenza GL; Thomas GH
Am J Med Genet; 2002 Apr; 109(2):133-8. PubMed ID: 11977162
[TBL] [Abstract][Full Text] [Related]
7. Deletion of chromosome 2q37 and autism: a distinct subtype?
Ghaziuddin M; Burmeister M
J Autism Dev Disord; 1999 Jun; 29(3):259-63. PubMed ID: 10425588
[TBL] [Abstract][Full Text] [Related]
8. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G
Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
[TBL] [Abstract][Full Text] [Related]
9. FISH-mapping of a 100-kb terminal 22q13 deletion.
Anderlid BM; Schoumans J; Annerén G; Tapia-Paez I; Dumanski J; Blennow E; Nordenskjöld M
Hum Genet; 2002 May; 110(5):439-43. PubMed ID: 12073014
[TBL] [Abstract][Full Text] [Related]
10. Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.
Lacbawan FL; White BJ; Anguiano A; Rigdon DT; Ball KD; Bromage GB; Yang X; DiFazio MP; Levin SW
Am J Med Genet; 1999 Nov; 87(2):139-42. PubMed ID: 10533028
[TBL] [Abstract][Full Text] [Related]
11. A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation.
Borg I; Squire M; Menzel C; Stout K; Morgan D; Willatt L; O'Brien PC; Ferguson-Smith MA; Ropers HH; Tommerup N; Kalscheuer VM; Sargan DR
J Med Genet; 2002 Jun; 39(6):391-9. PubMed ID: 12070244
[TBL] [Abstract][Full Text] [Related]
12. Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region.
Male A; Davies A; Bergbaum A; Keeling J; FitzPatrick D; Mackie Ogilvie C; Berg J
Eur J Hum Genet; 2002 Dec; 10(12):807-12. PubMed ID: 12461687
[TBL] [Abstract][Full Text] [Related]
13. Identification of the breakpoints at 1p36.2 and 3p21.3 in an AML(M3) patient who had t(1;3)(p36.2;p21.3) at the third relapse.
Tri NK; Xinh PT; Nagao H; Izumi T; Ozawa K; Toyoda A; Hattori M; Sakaki Y; Tokunaga K; Sato Y
Genes Chromosomes Cancer; 2002 Dec; 35(4):365-7. PubMed ID: 12378531
[TBL] [Abstract][Full Text] [Related]
14. The microcell hybrid-based "elimination test" identifies a 1-Mb putative tumor-suppressor region at 3p22.2-p22.1 centromeric to the homozygous deletion region detected in lung cancer.
Kholodnyuk ID; Kost-Alimova M; Yang Y; Kiss H; Fedorova L; Klein G; Imreh S
Genes Chromosomes Cancer; 2002 Jul; 34(3):341-4. PubMed ID: 12007195
[TBL] [Abstract][Full Text] [Related]
15. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
Van Roy N; Vandesompele J; Berx G; Staes K; Van Gele M; De Smet E; De Paepe A; Laureys G; van der Drift P; Versteeg R; Van Roy F; Speleman F
Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774
[TBL] [Abstract][Full Text] [Related]
16. Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletion.
Wolff DJ; Clifton K; Karr C; Charles J
Genet Med; 2002; 4(1):10-4. PubMed ID: 11839952
[TBL] [Abstract][Full Text] [Related]
17. [Genetics of autism].
Sedlácek Z; Havlovicová M; Hrdlicka M
Cas Lek Cesk; 2002 Jun; 141(12):376-80. PubMed ID: 12238023
[TBL] [Abstract][Full Text] [Related]
18. Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey.
Lauritsen M; Mors O; Mortensen PB; Ewald H
J Child Psychol Psychiatry; 1999 Mar; 40(3):335-45. PubMed ID: 10190335
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: cytogenetic and molecular investigation.
Nixon J; Oldridge M; Wilkie AO; Smith K
Am J Med Genet; 1997 Jun; 70(3):324-7. PubMed ID: 9188674
[TBL] [Abstract][Full Text] [Related]
20. Y chromosome haplogroups in autistic subjects.
Jamain S; Quach H; Quintana-Murci L; Betancur C; Philippe A; Gillberg C; Sponheim E; Skjeldal OH; Fellous M; Leboyer M; Bourgeron T
Mol Psychiatry; 2002; 7(2):217-9. PubMed ID: 11840316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]